课题基金 / 基金详情

项目摘要

项目成果

Katia Del Rio-Tsonis的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY When it comes to tissue regeneration in vertebrates the newts stand out as the champions. These animals can regenerate many organs and body parts even as adults and of old age. Thus, the newts could provide much coveted answers that the field of regenerative biology and medicine seeks. Among all tissues that can be regenerated the lens is a classic case of transdifferentiation because when removed as a whole regeneration ensues from a different tissue, the iris. Interestingly only the dorsal side of the iris is capable for transdifferentiation and not the ventral even though they both are made up of pigment epithelial cells. Thus, there must exist fundamental differences between dorsal and ventral iris that allow regeneration from the one site and not the other. Via transcriptomic analysis we have identified interesting patterns of gene expression. Some of the genes that show high levels of expression in dorsal or ventral iris will be examined in this proposal. In particular, we will examine the role of highly-regulated transcriptional factors in dorsal or ventral iris in the induction process (specific aim 1). For example, we have identified Tbx5 and Vax2 as dorsal- and ventral –specific respectively. Can the ventral iris be induced if we knock-down Vax2 or up-regulate Tbx5? Also we have seen interesting patterns of regulation of Ephrin-B2 and its receptor as well as of netrin-1 and its receptor UNC5 (specific aim 2). Ephrin-B2 is highly expressed in the dorsal iris, while netrin-1 in the ventral iris, with their receptors having opposite patterns. Since these pairs are involved in repulsion of cells we believe that they are involved in setting the boundaries between dorsal and ventral iris and disallow mingling of dorsal and ventral iris cells, thus ensuring correct regeneration. Moreover, it seems that Ephrin/netrin signaling is part of the Vax2/Tbx5 network, implying that all these genes might establish a novel pathway, which regulates lens regeneration. This will be investigated with gain- or loss-of-function experiments. Outcome of the proposed experiments will provide firm answers as to mechanisms of regeneration and will allow us to extend in other species with the ultimate goal to eventually induce lens regeneration in mammals.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A Roadmap to Uncover RPE Plasticity
  • 批准号:
    10639436
  • 项目类别:
  • 资助金额:
    $36.13万
  • 财政年份:
    2023
  • 负责人:
    Katia Del Rio-Tsonis
  • 依托单位:
Inflammation is a driver of newt lens regeneration
  • 批准号:
    10705582
  • 项目类别:
  • 资助金额:
    $18.06万
  • 财政年份:
    2022
  • 负责人:
    Katia Del Rio-Tsonis
  • 依托单位:
Inflammation is a driver of newt lens regeneration
  • 批准号:
    10433462
  • 项目类别:
  • 资助金额:
    $21.68万
  • 财政年份:
    2022
  • 负责人:
    Katia Del Rio-Tsonis
  • 依托单位:
In vivo imaging of newt lens regeneration: Novel molecular, cellular and functional insights
  • 批准号:
    10250409
  • 项目类别:
  • 资助金额:
    $17.52万
  • 财政年份:
    2020
  • 负责人:
    Katia Del Rio-Tsonis
  • 依托单位:
国内基金
海外基金
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
  • 依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    雷芬芳
  • 依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
    --
  • 项目类别:
    面上项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    万荣
  • 依托单位: